23080-22-0

Basic information

• Product Name: 2-(2-OXO-2-P-TOLYL-ETHYLSULFANYL)-1-P-TOLYL-ETHANONE
• Synonyms: 2-(2-OXO-2-P-TOLYL-ETHYLSULFANYL)-1-P-TOLYL-ETHANONE
• CAS NO: 23080-22-0
• Molecular Formula: C₁₈H₁₈O₂S
• Molecular Weight: 298.3993
• Mol File: 23080-22-0.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 470.1°Cat760mmHg
• Flash Point: 201.2°C
• Appearance: /
• Density: 1.148g/cm³
• CAS DataBase Reference: 2-(2-OXO-2-P-TOLYL-ETHYLSULFANYL)-1-P-TOLYL-ETHANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-OXO-2-P-TOLYL-ETHYLSULFANYL)-1-P-TOLYL-ETHANONE(23080-22-0)
• EPA Substance Registry System: 2-(2-OXO-2-P-TOLYL-ETHYLSULFANYL)-1-P-TOLYL-ETHANONE(23080-22-0)

Safety Data

• Hazardous Substances Data: 23080-22-0(Hazardous Substances Data)

Usage

Type of compound

Ketone

Groups present

Tolyl group, Ethylsulfanyl group

Uses

Pharmaceutical intermediate, Agrochemical intermediate, Material science research

Structure

Carbonyl group, Sulfur atom bonded to an ethyl group

Value

Building block for the synthesis of other organic compounds and materials

Properties and potential uses

Vary depending on specific conditions and applications

Upstream product

• 4209-24-9 p-methylphenacyl chloride 
• 619-41-0 4-(bromoacetyl)toluene 
• 98475-04-8 1-(4-methylphenyl)-2-(p-tolylsulfonyloxy)ethanone 
• 122-00-9 para-methylacetophenone 
• 108-88-3 toluene 

Downstream Products

• 69626-08-0 3,8-di-p-tolyl-2,5,6,7-tetrahydro-[1,4,7]thiadiazonine 
• 71764-43-7 1,2,3,4,9,9a-hexahydro-6,9a-di(p-methylphenyl)pyrimido<2,1-c><1,4>thiazine 
• 93876-77-8 3,4-di-p-tolylthiophene 
• 128592-65-4 1-(4-methylphenyl)-2-piperidino-2-thioxo-1-ethanone 
• 220102-36-3 1-(4-methylphenyl)-2-morpholino-2-thioxo-1-ethanone 
• 1393811-87-4 cis-2,6-di(4-methylphenyl)-1,4-oxathiane 
• 74794-44-8 (3-phenylthiene-2,5-diyl)bis[(4-tolyl)methanone] 
• 1391976-25-2 bis(4-methylphenylethynyl) sulfide 
• 107969-77-7 1,5-bis(4-methylphenyl)-3-phenylpentane-1,5-dione 
• 1400898-61-4 3-(4-chlorophenyl)-1-(4-methylphenyl)-5-phenyl-1,5-pentanedione 
• 1400898-63-6 1,3-di(4-chlorophenyl)-5-(4-methylphenyl)-1,5-pentanedione 

Relevant articles and documents

Synthesis of Thioethers Using Triethylamine-Activated Phosphorus Decasulfide (P410

The synthesis of thioethers in excellent yields was achieved under mild conditions via the displacement reaction of halogens by sulfur. The cross-reaction of 2-(α-bromoacetyl)thiophene with triethylamine-activated phosphorus decasulfide (Et3N-P2S5) was elaborated by utilizing DFT calculations.

Stereoselective synthesis of cis-2,6-disubstituted morpholines and 1,4-oxathianes by intramolecular reductive etherification of 1,5-diketones

A simple and efficient, Lewis acid catalysed reductive etherification strategy for the stereoselective synthesis of cis-2,6- disubstituted morpholines and 1,4-oxathianes starting from readily available 1,5-diketones has been developed. The strategy is used in the total synthesis of morpholine-based natural products (±)-chelonin A and formal total synthesis of (±)-chelonin C.

An aquatic pseudo-four-component reaction for the synthesis of highly substituted thiophenes

A novel and simple procedure was developed for the construction of fully substituted thiophenes. A series of α-haloacetophenone derivatives were converted into fully substituted thiophenes by treatment with sodium sulfide in the presence of 1,8-diazabicyc